Cite
HARVARD Citation
Lesage, S. et al. (2015). Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology. p. . [Online].
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Lesage, S. et al. (2015). Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology. p. . [Online].